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炎症基因变异作为预测炎症性肠病发生的分子标志物。

Variations in inflammatory genes as molecular markers for prediction of inflammatory bowel disease occurrence.

作者信息

Stankovic Biljana, Dragasevic Sanja, Popovic Dragan, Zukic Branka, Kotur Nikola, Sokic-Milutinovic Aleksandra, Alempijevic Tamara, Lukic Snezana, Milosavljevic Tomica, Nikcevic Gordana, Pavlovic Sonja

机构信息

Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Belgrade, Serbia.

Clinic for Gastroenterology and Hepatology, Clinical Center of Serbia, Belgrade, Serbia.

出版信息

J Dig Dis. 2015 Dec;16(12):723-33. doi: 10.1111/1751-2980.12281.

Abstract

OBJECTIVE

Research on inflammatory bowel disease (IBD) has highlighted genes involved in the regulation of inflammatory responses as contributors to disease pathogenesis. This study aimed to evaluate the associations between IBD and variations in NOD2, TLR4, TNF-α, IL-6, IL-1β and IL-1RN genes, and to use the genetic data obtained in predictive modeling.

METHODS

A total of 167 IBD patients and 101 healthy controls were genotyped by polymerase chain reaction-restriction fragment length polymorphism. Using the genotype data attained as the input to various classification algorithms, IBD prediction models were designed. The area under the receiver operating characteristic curve (AUROC) was used to measure their performance.

RESULTS

Significant associations were found between Crohn's disease (CD) and minor NOD2 variants, as well as TLR4 299Gly, TNF-α G-308A, IL-6 G-174C and IL-1RN VNTR A2 variants, while ulcerative colitis (UC) was associated only with IL-1RN VNTR A2 variants. CD and UC showed highly significant difference in the allelic distribution of TNF-α G-308A, where the A allele was found to be related to CD, and the G allele to UC. A combined effect of patients' gender and TLR4 variants was observed among CD patients. When all analyzed genotype and gender data were used, prediction performance achieved a maximum AUROC of 0.690 for CD and 0.601 for UC dataset.

CONCLUSION

Variations in the genes involved in immune regulation are genetic factors of importance in IBD susceptibility that could potentially be used as predictors of disease development.

摘要

目的

炎症性肠病(IBD)的研究突出了参与炎症反应调节的基因在疾病发病机制中的作用。本研究旨在评估IBD与NOD2、TLR4、TNF-α、IL-6、IL-1β和IL-1RN基因变异之间的关联,并将获得的基因数据用于预测模型。

方法

采用聚合酶链反应-限制性片段长度多态性方法对167例IBD患者和101例健康对照进行基因分型。以获得的基因型数据作为各种分类算法的输入,设计IBD预测模型。采用受试者工作特征曲线下面积(AUROC)来衡量其性能。

结果

发现克罗恩病(CD)与NOD2次要变异以及TLR4 299Gly、TNF-α G-308A、IL-6 G-174C和IL-1RN VNTR A2变异之间存在显著关联,而溃疡性结肠炎(UC)仅与IL-1RN VNTR A2变异相关。CD和UC在TNF-α G-308A的等位基因分布上存在高度显著差异,其中A等位基因与CD相关,G等位基因与UC相关。在CD患者中观察到患者性别和TLR4变异的联合效应。当使用所有分析的基因型和性别数据时,CD数据集的预测性能达到最大AUROC为0.690,UC数据集为0.601。

结论

参与免疫调节的基因变异是IBD易感性的重要遗传因素,有可能用作疾病发展的预测指标。

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